Summary of potential sEV-associated protein biomarkers for AD
AD sEVs protein biomarkers | Expression | References |
---|---|---|
Aβ42 | ↑ | [39, 56, 58, 59] |
P-T181-tau | ↑ | [56, 58] |
P-S396-tau | ↑ | [39, 56, 58, 59] |
T-tau | ↑ | [39, 58, 59] |
β-site APP cleaving enzyme 1 (BACE 1) | ↑ | [39] |
γ-Secretase | ↑ | [39] |
sAPPβ | ↑ | [39] |
sAPPα | ↑ | [39] |
Glial-derived neurotrophic factor (GDNF) | ↓ | [39] |
NRGN | ↓ | [57, 59] |
Repressor element 1-silencing transcription factor (REST) | ↓ | [59] |
GAP43 | ↓ | [57] |
Synaptotagmin 1 | ↓ | [57] |
SNAP25 | ↓ | [57] |
↑: the expression of the protein is higher in sEVs collected from samples of AD patients compared to that collected from controls; ↓: the expression of the protein is lower in sEVs collected from samples of AD patients compared to that collected from controls
SAA: Conceptualization, Writing—original draft. IC: Writing—original draft. KD: Writing—review & editing, Supervision. All authors read and approved the submitted version.
The authors declare that they have no conflicts of interest.
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KD is supported by the National Institute of General Medical Sciences of the National Institutes of Health under award number [1 R16GM149496-01]; and the National Science Foundation under award number [2302452]; funding was also provided by the North Carolina A&T State University KL2 Scholar Award from the National Center for Advancing Translational Sciences, National Institutes of Health, grant [KL2TR002490]; and start-up funds from the Joint School of Nanoscience and Nanoengineering, North Carolina A&T State University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
© The Author(s) 2024.